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3-(4-formyl-2-methoxyphenoxy)-4-hydroxy-5-methoxybenzaldehyde is a complex organic compound with the molecular formula C17H14O6. It is characterized by a benzaldehyde structure, which includes a benzene ring with an aldehyde group (-CHO) attached to the 4-position. The molecule also features a hydroxyl group (-OH) at the 4-position and a methoxy group (-OCH3) at the 5-position of the benzene ring. Additionally, it has a 2-methoxyphenoxy group attached to the 3-position, which itself contains a formyl group (-CHO) at the 4-position. 3-(4-formyl-2-methoxyphenoxy)-4-hydroxy-5-methoxybenzaldehyde is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds due to its diverse functional groups, which can participate in various chemical reactions.

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  • 2555-98-8 Structure
  • Basic information

    1. Product Name: 3-(4-formyl-2-methoxyphenoxy)-4-hydroxy-5-methoxybenzaldehyde
    2. Synonyms: 3-(4-formyl-2-methoxyphenoxy)-4-hydroxy-5-methoxybenzaldehyde
    3. CAS NO:2555-98-8
    4. Molecular Formula:
    5. Molecular Weight: 302.284
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2555-98-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-(4-formyl-2-methoxyphenoxy)-4-hydroxy-5-methoxybenzaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-formyl-2-methoxyphenoxy)-4-hydroxy-5-methoxybenzaldehyde(2555-98-8)
    11. EPA Substance Registry System: 3-(4-formyl-2-methoxyphenoxy)-4-hydroxy-5-methoxybenzaldehyde(2555-98-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2555-98-8(Hazardous Substances Data)

2555-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2555-98-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,5 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2555-98:
(6*2)+(5*5)+(4*5)+(3*5)+(2*9)+(1*8)=98
98 % 10 = 8
So 2555-98-8 is a valid CAS Registry Number.

2555-98-8Relevant articles and documents

NMR Assignment for Diaryl Ether Structures (4-O-5 Structures) in Pine Wood Lignin

Li, Yanding,Akiyama, Takuya,Yokoyama, Tomoya,Matsumoto, Yuji

, p. 1921 - 1929 (2016/07/06)

A 4-O-5-tetramer lignin model compound carrying β-O-4 linkages on each of the side-chain moieties was synthesized, as well as 4-O-5-coupled dehydrodiconiferyl alcohol. By comparison with their NMR data, two cross-signals in the HSQC spectrum of pine milled wood lignin recorded in DMSO-d6 were assigned to H2/C2 and H6/C6 correlations on the aromatic rings of 4-O-5-linked units. Although the H2/C2 correlation peak appeared in the same region as syringyl units, nitrobenzene oxidation of the pine lignin did not yield any syringyl-type product, but did release a 4-O-5-type product.

Structures of the radical (DPPH) oxidation products of dihydrocapsaicin

Nakamura, Tetsuya,Ooi, Takashi,Kogure, Kentaro,Nishimura, Miki,Terada, Hiroshi,Kusumi, Takenori

, p. 8181 - 8183 (2007/10/03)

Dihydrocapsaicin was oxidized with 2,2-diphenyl-1-picrylhydrazyl (DPPH), a free radical, and the products were analyzed by spectroscopic means.

Identification and Synthesis of New Ferulic Acid Dehydrodimers Present in Grass Cell Walls

Ralph, John,Quideau, Stephane,Grabber, John H.,Haffield, Ronald D.

, p. 3485 - 3498 (2007/10/02)

Seven isomeric dehydrodimers of ferulic acid (4-hydroxy-3-methoxycinnamic acid) have been synthesized and identified in extracts of saponified cell walls of cocksfoot, switchgrass, and suspension-cultured corn.Dehydrodimers (E,E)-4,4'-dihydroxy-5,5'-dimethoxy-3,3'-bicinnamic acid, trans-5--2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dihydrobenzofuran-3-carboxylic acid, (Z)-β--2-methoxyphenoxy>-4-hydroxy-3-methoxycinnamic acid, (E)-3--2-methoxyphenoxy>-4-hydroxy-5-methoxycinnamic acid, (E,E)-4,4'-dihydroxy-3,5'-dimethoxy-β,3'-bicinnamic acid, 4,4'-dihydroxy-3,3'-dimethoxy-β,β'-bicinnamic acid, and trans-7-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-6-methoxy-1,2-dihydronaphthalene-2,3-dicarboxylic acid, all arise from oxidative coupling of ferulate esters in cell walls and represent products of 8-5, 8-8, 8-O-4, 4-O-5, and 5-5 radical coupling.Prior literature has acknowledged only the presence of the 5-5 coupled dehydrodimer (E,E)-4,4'-dihydroxy-5,5'-dimethoxy-3,3'-bicinnamic acid.Consequently, by measuring only a single dehydrodimer and assuming inappropriate response factors, ferulate dehydrodimers have been underestimated by factors of up to 20.Synthetic routes to all seven isomers have been developed to provide structural authentication and determination of GC response factors.

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